What this pack is
COVERSYL is the brand name in this record; perindopril is the generic name. Read both together with the dosage form (oral tablet).
PACK CHECK · MARKET FIRST
Perindopril is converted to the active metabolite perindoprilat and inhibits angiotensin-converting enzyme, reducing angiotensin II- and aldosterone-related effects. This helps explain why blood pressure, kidney function, potassium and the complete medicine list matter, but neither the mechanism nor a blood-pressure number selects a salt, strength, tablet count, stop or combination for an individual.
Read source: Canada ↗Current regulatory record · reviewed 2026-08-29More about its action and precautions →A medicine may use different brand names across markets. Keep the market, brand, generic name, dosage form and route together; one matching field does not prove that two packs are the same or interchangeable.
Use these fields when the pack, market name or package image needs closer checking. They are evidence boundaries, not substitution instructions.
The evidence status and note below apply only to the stated market and source. They do not prove that packs in different markets can be substituted.
No source-verifiable mainland-China trade-name cue has been established for this record. This does not establish whether the medicine exists, is approved or is available in mainland China. Check pack text and current CDE/NMPA records item by item.
FOR EVERYDAY QUESTIONS
COVERSYL is the brand name in this record; perindopril is the generic name. Read both together with the dosage form (oral tablet).
This is a source-traceable public record. It helps you read the product identity and its listed source documents; each market still needs its own current record check.
Bring the actual pack, the label or prescription, and a complete medicine list when you speak with a pharmacist or clinician.
NEXT SAFE STEP
PRODUCT PRESENTATION IDENTITY
Package strength is not an individual dose. These fields help identify the exact labelled product; they do not calculate how much, how often, a missed-use action, splitting, switching or conversion.
First match the market, dosage form and labelled amount on the pack in hand. The number of tablets, sachets or devices in a pack is not a personal dose or schedule.
AU · TGA ARTG 101564 (verified 29 Aug 2026)
Source-text identity card: no displayable exact official package image. The fields below come from the cited label and are not a visual authentication result.
AU · TGA ARTG 101568 (verified 29 Aug 2026)
Source-text identity card: no displayable exact official package image. The fields below come from the cited label and are not a visual authentication result.
AU · TGA ARTG 101569 (verified 29 Aug 2026)
Source-text identity card: no displayable exact official package image. The fields below come from the cited label and are not a visual authentication result.
PACKAGE-VISUAL STATUS
TGA product pages verify brand, salt, strength per tablet, ARTG, form and bottle presentation but do not provide a public principal-display image mapped one-to-one to all three products. The Canadian monograph supplies tablet colour, shape and packaging text clues, but these cannot stand in for Australian appearance. The page therefore discloses the image gap and shows traceable identity cards only.
LABEL READING · NOT A PRESCRIPTION
Reading level: drug-specific label reading. This record has been expanded around its dosage form or a higher-risk reading question; the current target-market label and professional review still apply.
Australia and Canada both use the COVERSYL brand, but their official records use different salts and milligram numbers. A shared brand or active moiety does not permit self-conversion from the numbers. This page only helps check the exact pack, market and current label; it calculates no individual's tablet count, frequency, start, stop, addition or switch.
PHARMACOVIGILANCE · OFFICIAL ROUTES
Start with the public label or product record linked to this dossier, then use the official safety routes below for the market that applies to the medicine in hand.
This checklist only helps organise the right question. It does not create a personal conclusion about stopping, switching, dose, combination or suitability.
This dossier’s publicly accessible product-level route has been checked individually. It does not mean that real-time alerts in every country or region have been searched, or that the medicine has or does not have a current risk.
This is a document-coverage summary, not a claim that the medicine is authorised, supplied, interchangeable or actively monitored in every listed market today.
These are separately reviewed product documents for the same dossier. Their market, date, dosage form and document status must stay attached to each link; they do not establish interchangeability between products, strengths, packs, indications or countries.
This is not a conclusion that the medicine has no risk, warning, recall or newer notice in another market. Start with the checked product-level label above, then use the official market gateways below for the product in hand.
See the reviewed safety-record directory →This card brings together the medicine-specific product route and 15 market-level official vigilance gateways. It does not mean real-time alerts for this medicine have been searched in every country or region, or that the medicine has a new alert, recall or risk conclusion. Match brand, generic name, dosage form, strength, market and notice date item by item; do not self-stop, switch, increase or reduce use from a headline.
For severe or rapidly worsening symptoms, suspected overdose, a severe allergic reaction, loss of consciousness or another emergency, use local emergency services. Do not wait for an online alert search or change a medicine from this page.
PRIVATE FAMILY LIST
Only the brand, generic name, dosage form and route are added, and they stay in this browser. Copy strength, label directions, start/stop history and any concern from the actual pack; this tool does not calculate a dose or decide combination, switching or stopping.
Add to the family medicine list →PACK · LABEL · MEDICINE LIST
Use this card to organise questions about COVERSYL (perindopril). Keep the exact pack, its current label and the full medicine list together.
COVERSYL is the brand in this record and perindopril is the active-ingredient name. Check both with the dosage form (Perindopril oral tablets: Australian arginine 2.5/5/10 mg and Canadian-monograph erbumine 2/4/8 mg; the page provides no salt or milligram conversion) and the market on the actual pack.
mg, mcg, mg/mL or a percentage describes the labelled amount in one tablet, capsule, measured volume, spray or other unit. It is not an answer to how many units a person should take.
Before splitting, crushing, chewing or opening anything, find an explicit instruction for this exact product in its current label and ask a pharmacist. A score line or a previous pack is not enough by itself.
Include prescriptions, over-the-counter products, eye drops, creams, vitamins, minerals, herbs and supplements. A pharmacist or prescriber needs the whole list before any combination, alternation, switch or stop is considered.
Ask which medicine, which gene and what clinical decision a result could change. A gene–drug association does not mean broad genetic testing is needed for everyone and must not be used to change treatment without professional review.
For a suspected overdose, a severe allergic reaction, fainting or difficulty breathing, use the local emergency or poison-information service now. Do not wait for a website reply or alter several medicines to test what caused it.
This card does not calculate a dose, decide whether medicines can be combined, or replace a clinician or pharmacist. Market-specific current labels and the person's full context still need review.
MARKET DOCUMENTS · READ SEPARATELY
Each link retains its own market, date, dosage form and document status. These documents support larger-print reading and item-by-item checking; they do not make products, strengths, packs, indications or use between countries or regions interchangeable.
HOW IT WORKS · NOT A TREATMENT PLAN
SOURCE EVIDENCE REGISTER
Every public link is labelled with its market, document status and document type. A historical public record is not a current label, and an official lookup entry is not a product-specific record.
SOURCE-TRACEABLE ARCHIVE
This page links to public primary-source material for COVERSYL. The archive is historical or documentary evidence only; it does not by itself establish originator status, product quality, current labelling, availability or sale eligibility.
DOCUMENT TIMELINE
The current Health Canada page lists COVERSYL perindopril erbumine 4 mg tablets, DIN 02123282, as marketed. This does not establish stock at a particular pharmacy.
Health Canada: current Drug Product Database (DPD) access page; search COVERSYL 4 mg / DIN 02123282 in the database ↗TGA separately lists 2.5, 5 and 10 mg tablet bottles under ARTG 101564, 101568 and 101569 with licence status A.
Australian TGA: COVERSYL perindopril arginine 10 mg tablet bottle (ARTG 101569) ↗The monograph lists appearance, packaging, warnings, interactions and patient information for erbumine 2, 4 and 8 mg tablets; it does not convert those numbers into Australian arginine strengths.
Health Canada: current COVERSYL perindopril erbumine product monograph and patient information (21 Oct 2022) ↗MARKET SCOPE
A regulatory record does not establish pharmacy stock, purchasing eligibility, individual suitability or self-switching.
The current monograph covers 2, 4 and 8 mg tablets; actual supply and pack still require exact-product review.
No local trade name, approval, salt, pack, supply, originator/generic relationship or interchangeability is inferred from Australian or Canadian records.
Read each document in its stated market, date and dosage-form context. A historical record is not a current label and does not support individual medical, substitution or purchasing conclusions.
RECORD FAQ
Do not decide from brand or number alone. The Australian record is 5 mg arginine, while the Canadian monograph is 4 mg erbumine. This site provides no self-conversion or substitution rule; have the exact salt, pack, prescription and target-market label reviewed.
A score is first an appearance-identification clue, not universal splitting permission. Salt, strength, market and manufacturer may differ; follow the current label for the exact product and professional instruction.
No. The former also contains indapamide and the latter amlodipine. Check every ingredient to avoid duplication with single-ingredient perindopril, diuretics, amlodipine or other blood-pressure medicines; do not self-disassemble, combine or substitute.
READ NEXT
The listed links are public sources selected for traceability. They must be rechecked against the current target-market record before any use beyond reading and research.